美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
63187-590-09	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20260513	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (63187-590-09)
63187-590-14	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240904	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (63187-590-14)
63187-590-20	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63187-590-20)
63187-590-30	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-590-30)
63187-590-60	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-590-60)
63187-590-72	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (63187-590-72)
63187-590-90	63187-590	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA078722	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-590-90)